Camiña-Tato M - Search Results

1

Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms.

Comabella M, Craig DW, Camiña-Tato M, Morcillo C, Lopez C, Navarro A, Rio J; BiomarkerMS Study Group; Montalban X, Martin R. Comabella M, et al. Among authors: camina tato m. PLoS One. 2008;3(10):e3490. doi: 10.1371/journal.pone.0003490. Epub 2008 Oct 22. PLoS One. 2008. PMID: 18941528 Free PMC article.

2

Genetic association between polymorphisms in the BTG1 gene and multiple sclerosis.

Camiña-Tato M, Morcillo-Suárez C, Navarro A, Fernández M, Horga A, Montalban X, Comabella M. Camiña-Tato M, et al. J Neuroimmunol. 2009 Aug 18;213(1-2):142-7. doi: 10.1016/j.jneuroim.2009.05.010. Epub 2009 Jun 9. J Neuroimmunol. 2009. PMID: 19515430

3

Genetic association of CASP8 polymorphisms with primary progressive multiple sclerosis.

Camiña-Tato M, Fernández M, Morcillo-Suárez C, Navarro A, Julià E, Edo MC, Montalban X, Comabella M. Camiña-Tato M, et al. J Neuroimmunol. 2010 May;222(1-2):70-5. doi: 10.1016/j.jneuroim.2010.03.003. Epub 2010 Apr 2. J Neuroimmunol. 2010. PMID: 20363033

4

Gender-associated differences of perforin polymorphisms in the susceptibility to multiple sclerosis.

Camiña-Tato M, Morcillo-Suárez C, Bustamante MF, Ortega I, Navarro A, Muntasell A, López-Botet M, Sánchez A, Carmona P, Julià E, Tortola MT, Audí L, Oksenberg JR, Martin R, Montalban X, Comabella M. Camiña-Tato M, et al. J Immunol. 2010 Nov 1;185(9):5392-404. doi: 10.4049/jimmunol.1000102. Epub 2010 Oct 4. J Immunol. 2010. PMID: 20921521

5

A type I interferon signature in monocytes is associated with poor response to interferon-beta in multiple sclerosis.

Comabella M, Lünemann JD, Río J, Sánchez A, López C, Julià E, Fernández M, Nonell L, Camiña-Tato M, Deisenhammer F, Caballero E, Tortola MT, Prinz M, Montalban X, Martin R. Comabella M, et al. Among authors: camina tato m. Brain. 2009 Dec;132(Pt 12):3353-65. doi: 10.1093/brain/awp228. Brain. 2009. PMID: 19741051

6

No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish population.

Fachal L, Mosquera-Miguel A, Pastor P, Ortega-Cubero S, Lorenzo E, Oterino-Durán A, Toriello M, Quintáns B, Camiña-Tato M, Sesar A, Vega A, Sobrido MJ, Salas A. Fachal L, et al. Among authors: camina tato m. Am J Med Genet B Neuropsychiatr Genet. 2015 Jan;168B(1):54-65. doi: 10.1002/ajmg.b.32276. Epub 2014 Oct 28. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 25349034

7

Synaptotagmin XI in Parkinson's disease: New evidence from an association study in Spain and Mexico.

Sesar A, Cacheiro P, López-López M, Camiña-Tato M, Quintáns B, Monroy-Jaramillo N, Alonso-Vilatela ME, Cebrián E, Yescas-Gómez P, Ares B, Rivas MT, Castro A, Carracedo A, Sobrido MJ. Sesar A, et al. Among authors: camina tato m. J Neurol Sci. 2016 Mar 15;362:321-5. doi: 10.1016/j.jns.2016.02.014. Epub 2016 Feb 8. J Neurol Sci. 2016. PMID: 26944171

8

mtDNA nt13708A variant increases the risk of multiple sclerosis.

Yu X, Koczan D, Sulonen AM, Akkad DA, Kroner A, Comabella M, Costa G, Corongiu D, Goertsches R, Camina-Tato M, Thiesen HJ, Nyland HI, Mørk SJ, Montalban X, Rieckmann P, Marrosu MG, Myhr KM, Epplen JT, Saarela J, Ibrahim SM. Yu X, et al. Among authors: camina tato m. PLoS One. 2008 Feb 13;3(2):e1530. doi: 10.1371/journal.pone.0001530. PLoS One. 2008. PMID: 18270557 Free PMC article.

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